Canonical Allele Identifier: CA428873551
Gene: PROC HGNC NCBI

Linked Data

dbSNP Id: rs1326161531

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127423080C>T , CM000664.2:g.127423080C>T GRCh38
NC_000002.11:g.128180656C>T , CM000664.1:g.128180656C>T GRCh37
NC_000002.10:g.127897126C>T NCBI36
NG_016323.1:g.9661C>T , LRG_599:g.9661C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000234071.8:c.309C>T MANE Select ENSP00000234071.4:p.Ser103=
ENST00000234071.7:c.309C>T ENSP00000234071.3:p.Ser103=
ENST00000409048.1:c.309C>T ENSP00000386679.1:p.Ser103=
ENST00000419985.5:c.*115C>T ENSP00000392606.1:n.*115C>T
ENST00000427769.5:c.309C>T ENSP00000406295.1:p.Ser103=
ENST00000429925.5:c.309C>T ENSP00000412697.1:p.Ser103=
ENST00000431364.1:c.*115C>T ENSP00000391220.1:n.*115C>T
ENST00000442644.5:c.309C>T ENSP00000411241.1:p.Ser103=
ENST00000474030.5:n.484C>T
NM_000312.3:c.309C>T , LRG_599t1:c.309C>T NP_000303.1:p.Ser103=
XM_005263715.3:c.492C>T XP_005263772.1:p.Ser164=
XM_005263716.3:c.372C>T XP_005263773.1:p.Ser124=
XM_005263717.3:c.372C>T XP_005263774.1:p.Ser124=
XM_005263717.4:c.372C>T XP_005263774.1:p.Ser124=
XM_017004505.1:c.552C>T XP_016859994.1:p.Ser184=
XM_024453002.1:c.552C>T XP_024308770.1:p.Ser184=
XM_024453003.1:c.492C>T XP_024308771.1:p.Ser164=
XM_024453004.1:c.492C>T XP_024308772.1:p.Ser164=
XM_024453005.1:c.372C>T XP_024308773.1:p.Ser124=
XM_024453006.1:c.309C>T XP_024308774.1:p.Ser103=
NM_000312.4:c.309C>T MANE Select NP_000303.1:p.Ser103=
NM_001375602.1:c.492C>T NP_001362531.1:p.Ser164=
NM_001375603.1:c.372C>T NP_001362532.1:p.Ser124=
NM_001375604.1:c.372C>T NP_001362533.1:p.Ser124=
NM_001375605.1:c.309C>T NP_001362534.1:p.Ser103=
NM_001375606.1:c.464C>T NP_001362535.1:p.Ala155Val
NM_001375607.1:c.393C>T NP_001362536.1:p.Ser131=
NM_001375608.1:c.309C>T NP_001362537.1:p.Ser103=
NM_001375609.1:c.285C>T NP_001362538.1:p.Ser95=
NM_001375610.1:c.303C>T NP_001362539.1:p.Ser101=
NM_001375611.1:c.309C>T NP_001362540.1:p.Ser103=
NM_001375613.1:c.309C>T NP_001362542.1:p.Ser103=